Isopropylamine → HCID 14813588, compound
Reaction equation
[CH:1]([NH2:4])([CH3:3])[CH3:2].Cl[P:6](Cl)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1>C(OCC)C>[CH:1]([NH:4][P:6]([NH:4][CH:1]([CH3:3])[CH3:2])[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of isopropylamine (30 ml, 352 mmol) in diethyl ether (250 ml), dichlorophenylphosphine (9.63 ml, 71 mmol, dissolved in 50 ml diethylether) was added at 0° C. over a period of 30 min. After stirring for a total of 72 hrs the solution was filtered. The residue was washed with diethylether and the solvent was removed in vacuum. The remaining oil was distilled at 0.2 Torr/76-78° C. to give a colorless liquid with 33% yield (5.3 g). 31P {H} NMR: 49.0 ppm.
Workup
- filtrationwas filtered
- washThe residue was washed with diethylether
- customthe solvent was removed in vacuum
- distillationThe remaining oil was distilled at 0.2 Torr/76-78° C.
- customto give a colorless liquid with 33% yield (5.3 g)
Sources & evidence
- ORD record
- ord-5605adf5416746c6a9db4695b1c38119
- Source dataset
- uspto-grants-2015_12
- Patent number
- US09221856B2
Reaction notes
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